"Pachyonychia Congenita" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A group of inherited ectodermal dysplasias whose most prominent clinical feature is hypertrophic nail dystrophy resulting in PACHYONYCHIA. Several specific subtypes of pachyonychia congenita have been associated with mutations in genes that encode KERATINS.
| Descriptor ID |
D053549
|
| MeSH Number(s) |
C16.131.831.350.856 C16.320.850.250.856 C17.800.529.594 C17.800.804.350.856 C17.800.827.250.856
|
| Concept/Terms |
Pachyonychia Congenita, Type 2- Pachyonychia Congenita, Type 2
- Pachyonychia Congenita, Jackson-Lawler Type
- Pachyonychia Congenita, Jackson Lawler Type
- Type 2 Pachyonychia Congenita
- Jackson-Lawler Type Pachyonychia Congenita
- Jackson Lawler Type Pachyonychia Congenita
Pachyonychia Congenita, Type 1- Pachyonychia Congenita, Type 1
- Pachyonychia Congenita, Jadassohn-Lewandowsky Type
- Pachyonychia Congenita, Jadassohn Lewandowsky Type
- Pachyonychia Congenita Tarda, Type 1
- Jadassohn-Lewandowsky Syndrome
- Jadassohn Lewandowsky Syndrome
- Pachyonychia Congenita Type 1
- Type 1 Pachyonychia Congenita
|
Below are MeSH descriptors whose meaning is more general than "Pachyonychia Congenita".
Below are MeSH descriptors whose meaning is more specific than "Pachyonychia Congenita".
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Below are the most recent publications written about "Pachyonychia Congenita" by people in Profiles.